Chitra s nayak 302 arun, 6th road, santacruz east, mumbai400 055 india. The patient was treated with diseasemodifying antirheumatic drugs dmards and aspirin for. A previous biopsy for histopathology was wrongly interpreted. Unilateral presentation of pseudokaposis secondary to superficial venous insufficiency clin dermatol j.
Acroangiodermatitis, often known as pseudokaposi sarcoma, is an. Histopathological examination from one of the lesions showed hyperplastic. An 18yearold male presented with a nonhealing wound on left lower limb, pain and swelling over multiple joints, weight loss, and yellowish discoloration of eyes and urine for the past 4 years. Methods and protocols provides a comprehensive guide to the current issues in histopathology. With chapters on organbased approaches with specific protocols for morphologic, molecular examination, and pathological observations governing the therapeutic management of the diseases. Acroangiodermatitis of mali, chronic venous insufficiency, pseudokaposi. Thus, the histopathology confirmed acroangiodermatitis of mali. Mali described the characteristic lesions as peculiar purple macular plaques on the extensor aspects of the digits or foot. We report a 17yearold girl with congenital spina bifida and myelomeningocele and cutaneous lesions localized on the lower limbs. There are 0 terms under the parent term acroangiodermatitis in the icd10cm alphabetical index.
It appears to be a reactive phenomenon related to severe chronic venous insufficiency and stasis of the lower extremities. On examination, the patient had pallor, icterus, and generalized lymphadenopathy with a nonhealing unhealthy ulcer over left medial malleolus. Acroangiodermatitis of mali resulting from arteriovenous malformation. To achieve this it is important that the tissue must be prepared in such a manner. A rare vascular phenomenon arpita a mehta, rickson r pereira, chitra s nayak, rachita s dhurat department of dermatology, t. Kaposilike acroangiodermatitis or pseudokaposis sarcoma is a reactive angiodysplasia of the cutaneous blood vessels that resembles true kaposis sarcoma, both clinically and histologically. Histopathology techniques histopathology definition. Department of histopathology, south warwickshire general hospital, west midlands, uk. Acroangiodermatitis of mali george 2010 clinical and.
Stewartbluefarb syndrome is a variant of acroangiodermatitis, which is associated with congenital av malformationfistulas. Department of histopathology postgraduate institute of medical education and research, chandigarh, india. Results of the histopathologic analysis indicated ac roangiodermatitis. Although benign, it must be differentiated from malignant conditions like kaposis sarcoma, especially in the present hiv era and therefore, histopathological examination is. In more advanced, tumorous stages of kaposis sarcoma, cellular atypia becomes apparent and allows differentiation between malis acroangiodermatitis and true kaposis sarcoma. Acroangiodermatitis aad is a rare benign vascular proliferation characterized by violaceous patches or plaques of the extremities resembling kaposi sarcoma. Fixation, tissue processing, histologyand immunohistochemistry procedures for diagnosis of animal tse bse, scrapie, atypical scrapie,cwd pathology department, apha. The term acroangio dermatitis was introduced in 1965 by mali et al.
Pathology of acroangiodermatitis pseudokaposis sarcoma. Pseudokaposi sarcoma acroangiodermatitis treatment. Acroangiodermatitis is a reactive dermal capillary proliferation that occurs on the lower extremities of patients with severe chronic venous insufficiency mali type 58 or congenital arteriovenous malformations stewartbluefarb syndrome. Our patient had a case of mali type acroangiodermatitis beginning at a young er age in contrast to the most frequent cases, and it occurred unilaterally. Before presentation, he had also developed similar smaller superficial lesions below this area. On histopathology, papules and nodules consist of a proliferation of small dilated vessels in an edematous dermis.
Acroangiodermatitis of mali also called as pseudokaposi s sarcoma is a very rare, benign condition which clinically presents as purplecolored patches, plaques or nodules, mostly on the extensor. It is a proliferation of preexisting vasculature seen in chronic venous insufficiency, arteriovenous malformation, or acquired iatrogenic arteriovenous av fistula. First type namely the mali type of acroangiodermatitis is related to chronic venous insuffiency and second the stewartbluefarb type is associated with arteriovenous malformations. Acroangiodermatitis of mali in a patient with congenital myopathy. The diagnosis was confirmed using histopathological and. The authors report a case of acroangiodermatitis of mali type of the bilateral legs that was misdiagnosed for 3 years.
Acroangiodermatitis of mali stewartbluefarb syndrome acroangiodermatitis is a benign vascular process which histologically closely resembles kaposis sarcoma and had thus been named pseudokaposis sarcoma. Histopathological techniques histopathology is the branch of pathology which concerns with the demonstration of minute structural alterations in tissues as a result of disease. Acroangiodermatitis of mali in protein c deficiency due to a novel proc gene mutation. It would be difficult to propose a system for histopathology and anatomical pathology services applicable to all developing countries.
He had deformed joints with hepatomegaly and splenomegaly. Although benign, it must be differentiated from malignant conditions like kaposis sarcoma, especially in the present hiv era and therefore, histopathological examination is a must for its diagnosis and differentiation. The cases presented here demonstrate 2 potential variants of aad. Acroangiodermatitis secondary to chronic venous insufficiency see erratum 2011. Histopathological examination of the lesion showed lobular proliferation of small. The icd10cm alphabetical index is designed to allow medical coders to look up various medical terms and connect them with the appropriate icd codes. Apr 01, 2010 acroangiodermatitis of mali george, m carr, r. To achieve this it is important that the tissue must be prepared in such a manner that it is sufficiently thick or thin to be examined microscopically and all. Mali type acroangiodermatitis begins in the form of violaceus macules and patches, and it can transform into painless papulonodules or persistent plaques. Most of histopathological techniques simulating to those of. Histology page 1 histological techniques histology is the study of the cellular organization of body tissues and organs. Dermis acroangiodermatitis mali information on the diagnosis.
Acroangiodermatitis or pseudokaposi sarcoma is a rare angioproliferative entity, related to chronic venous insuf. Dermis acroangiodermatitis mali information on the. Acroangiodermatitis of stewartbluefarb poses a diagnostic dilemma with ks and klippeltrenaunay syndrome kts. Acroangiodermatitis of mali is a rare cutaneous condition often characterized by purplishblue to brown papules and plaques on the medial and lateral malleolus of both legs 1604 acroangiodermatitis is a rare skin condition characterised by hyperplasia of preexisting vasculature due to venous hypertension from severe chronic venous stasis. Malitype acroangiodermatitis begins in the form of violaceus macules and patches, and it can transform into painless papulonodules or persistent plaques. Acroangiodermatitis pseudokaposis sarcoma associated with klippeltrenaunay syndrome. Our patient had a case of malitype acroangiodermatitis beginning at a young er age in contrast to the most frequent cases, and it occurred unilaterally.
Capillary proliferation an overview sciencedirect topics. Hornick md, phd, in practical soft tissue pathology. The tissue undergoes a series of steps before it reaches the examiners desk to be thoroughly examined microscopically to arrive at a particular diagnosis. Histopathologists provide diagnostic expertise and advice for clinical colleagues, and work in clinical teams that care for patients. The term is derived from the greek histos meaning web or tissue, and refers to the science of tissues. Nonhea lc arly set nilateral ality acroangiodermatitis. View the article pdf and any associated supplements and figures for a period of 48 hours. The clinical and histopathological lesions resembled kaposis sarcoma. It has been described in patients with increased venous pressure and stasis caused by venous insufficiency, congenitalacquired arteriovenous mali et al.
Two years later, bluefarb and adams 10 described kaposiform skin lesions in one patient with a congenital arteriovenous malformation without chronic venous. The major advantages of histopathology are speed, low cost and the ability to provide a presumptive identification of the infecting fungus as well as demonstrating the tissue reaction. Histopathology in ks there is a proliferation of neoplastic spindle cells forming clefts and cavernous formations independent of preexisting vessels with presence of atypical cells while in acroangiodermatitis there is reactive proliferation of preexisting. It is a branch of pathology which deals with the study of disease in a tissue section.
Acroangiodermatitis of mali and stewartbluefarb syndrome. Chapter 1 introducton histopathology definition it is a branch of pathology which deals with the study of disease in a tissue section. Histopathology of both the cases showed dilated capillaries in the dermis with extravasated red. Kaposi sarcoma and requires histopathological examination for its diagnosis. Mar 03, 2014 acroangiodermatitis pseudokaposis sarcoma, coined by mali et al 12 in 1965, is described as a rare skin disease characterized by the presence of hyperplasia of preexisting vasculature. Acroangiodermatitis of mali acroangiodermatitis of mali george, m carr, r. Such an ulcer must undergo a biopsy so that an appropriate diagnosis can be reached and treatment instituted rapidly acroangiodermatitis of mali is an uncommon but not rare cause of nonhealing wound in the lower limbs. Acroangiodermatitis of mali stewartbluefarb syndrome acroangiodermatitis is a benign vascular process which histologically closely resembles kaposis sarcoma and had thus been named pseudokaposis sarcoma acroangiodermatitis is often associated with different disorders like.
To provide a standardized method for the appropriate filing andor retrieval of avoid being destroyed or eaten by pets. Acroangiodermatitis aad is a rare vasoproliferative disorder, usually of the lower. Acroangiodermatitis, often known as pseudokaposi sarcoma, is an uncommon angioprolifera tive entity related to chronic venous insufficiency, arteriovenous fistulae, paralysed limbs, amputation. Histopathology revealed expansion of the capillary bed that showed reduplication and corkscrewing as well as erythrocyte extravasation, fibrosis, and hemosiderin deposit figures 2, 3, and 4. Summary acroangiodermatitis synonym pseudo kaposi sarcoma. It is a proliferation of preexisting vasculature seen in venous hypertension, arteriovenous malformation, or acquired iatrogenic arteriovenous av fistula. Acroangiodermatitis is a reactive angiodysplasia of cutaneous blood vessels. With chapters on organbased approaches with specific protocols for morphologic, molecular examination, and pathological observations governing the therapeutic management of. Acroangiodermatitis synonym pseudokaposi sarcoma is an unusual, benign condition which clinically presents as purplecolored patches, plaques or nodules, mostly on the extensor surfaces of lower extremities in patients with chronic venous insufficiency and arteriovenous malformations. Acroangiodermatitis of mali is a rare cutaneous condition often characterized by purplishblue to brown papules and plaques on the medial and lateral malleolus of both legs. Acroangiodermatitis of mali pseudokaposi sarcoma associated. Acroangiodermatitis pseudokaposis sarcoma, coined by mali et al 12 in 1965, is described as a rare skin disease characterized by the presence of hyperplasia of preexisting vasculature. It usually begins early in life, unilaterally over lower extremities presenting as. The tissue undergoes a series of steps before it reaches the diagnosis.
Acroangiodermatitis is a benign uncommon vasoproliferative disorder that affects the lower extremities. Acroangiodermatitis, dermite ocre of favre, gravitational purpura, purpura, stasis, stasis purpura. Try out the html to pdf api handling of histopathology materials. Acroangiodermatitis pseudokaposi sarcoma acroangiodermatitis is a reactive dermal capillary proliferation that occurs on the lower extremities of patients with severe chronic venous insufficiency mali type 58 or congenital arteriovenous malformations stewart. The term acroangiodermatitis of mali was introduced for the first time by mali et al. Acroangiodermatitis mali resulting from arteriovenous malformation. Parkes weber syndrome pws is a rare disorder characterised by arteriovenous av fistula, along with capillary, lymphatic, venous malformations and limb hypertrophy.
Case of bilateral acroangiodermatitis due to symmetrical arteriovenous fistulas of the soles. Spontaneous acroangiodermatitis coban i, kokenekunal td. Nonhealing ulcer is a cause for significant morbidity and mortality. Unilateral presentation of pseudokaposis secondary to.
The histopathology laboratory has a policy for retention of materials in compliance with the college of american pathologist. Claudy, expression of the cd34 antigen distinguishes kaposis sarcoma from pseudokaposis sarcoma acroangiodermatitis, the british journal of. Acroangiodermatitis of mali in a patient with congenital. Histopathology remains one of the major tools of diagnosis in mycology20 table 3.